Metabolism and Mass Balance in Rats Following Oral Administration of the Novel Antifibrotic Drug Fluorofenidone

Introduction

Fluorofenidone (AKF-PD) is a novel antifibrotic small-molecule compound^1–3 that is the structural analog of pirfenidone.^4–6 Previous studies of the metabolic pathway of AKF-PD (see Figure 1) have found that there are two main metabolites of AKF-PD in rats:^7–12 methyl hydroxylation (M1) and carboxylated (M2) products of AKF-PD.¹³ Based on the structural formula of AKF-PD, combined with the theory of drug metabolism and reference to the metabolic pathway of the homologous compound pirfenidone, a possible metabolic pathway can be predicted (see Figure 1). In the present study, after intragastric administration of AKF-PD to rats, samples of urine and feces were collected for the extraction of metabolites; the metabolite content was then determined in order to study the mass balance of AKF-PD.

Figure 1 The metabolic pathway of AKF-PD.

Materials and Methods

Chemicals

AKF-PD (batch no.: 070701, content: 99.9%), AKF-PD hydroxylated metabolites (M1, batch no.: 070930, content: 93.0%), AKF-PD carboxylic metabolites (M2, batch no.: 070715, content: 97.8%), and carboxylated pirfenidone (batch no.: 070511, content: 99.8%) were provided by the School of Pharmacy, Central South University. Methanol (batch no.: 707108) and formic acid (batch no.: 409101) were of analytical or high-performance liquid chromatography (HPLC) grade and were supplied by Tedia, USA. Sodium carboxymethyl cellulose (CMC-Na) (batch no.: 031021) was supplied by Shantou Xilong Chemical Factory, China. Purified water was supplied by Hangzhou Wahaha Group Co., Ltd, China.

Experimental Animals

Sprague–Dawley (SD) rats of both genders with a mean weight of 160–200 g were provided by the Department of Experimental Animal Science, Central South University, license no.: SCXK (Hunan) 2006-0002.

Study Design

Fourteen SD rats (seven male and seven female) were placed in metabolic cages for three days. Their feed was ground into powder, and each rat was fed 25 ± 2 g per day and given water freely. Blank urine and fecal samples of SD rats for 24h before administration were collected on the night of the third day, followed by fasting for 12h. On the morning of the fourth day, each rat was given a single gavage (120 mg), and then the urine and fecal samples of rats 24h after administration were collected.

Administration of AKF-PD and the Determination of AKF-PD and Its Hydroxylated Metabolites (M1) in Rat Urine

The AKF-PD was crushed through a 100-mesh sieve, and 0.12 g was accurately weighed and placed into a 5 mL syringe. A total of 2 mL 0.5% CMC-Na aqueous solution was added and mixed with the crushed AKF-PD. After that, the mixture was administered to the rats via gavage, and the remaining part of the syringe was washed out with methanol into a 250 mL volumetric flask (Tables 1 and 2). Water was added to the scale, which was shaken well. A total of 100 µL of this solution was added to 400 µL of internal standard carboxylated pirfenidone acetonitrile solution (5µg/mL) and mixed well. And 10ul mixing was used for the simultaneous detection of AKF-PD and its hydroxylated metabolites (M1) in rat urine samples by HPLC-UV. After that, the detection of the residual amount of AKF-PD in order to calculate an accurate dosage.

Table 1 The Number, Basic Condition and Dosage of Each Tested Animal

Table 2 Dosage and Measurement of Residual Flufenidone After Administration

Sample Collection

After administration, urine samples at 0–3, 3–6, 6–10, 10–14, 14–24, 24–48, and 48–72 hours and feces samples at 0–24, 24–48, and 48–72 hours were collected. Before each collection, the collection funnel was rinsed with approximately 3 mL of 95% ethanol. After the rinsing solution was mixed with urine, the volume was measured and the urine samples were stored at –20°C. The feces were dried at 40°C for 12 hours and stored at room temperature, and they were weighed before measurement.

Analysis of the Urine and Feces Samples

Determination of AKF-PD and Its Carboxylated Metabolites (M2) in Rat Urine

HPLC-UV Conditions

Chromatographic conditions: HPLC ultraviolet detector (Agilent 1200 with Workstation B.03.01); chromatographic column (Synergi™ 4 µm Hydro-RP 80 Å 250×4.6 mm, Phenomenex); mobile phase: acetonitrile: 0.1% formic acid aqueous solution= 14.5:85.5(v/v) (0–22 mins), acetonitrile: 0.1% formic acid aqueous solution= 90:10 (v/v) (22.1–25 mins), acetonitrile: 0.1% formic acid aqueous solution= 14.5:85.5 (v/v) (25.1–29 mins); flow rate 1.0 mL/min; wavelength 310 nm; injection volume 10 µL.

Sample Pretreatment

A total of 100 µL of rat urine was added to 400 µL of methanol solution of carboxylated pirfenidone (25µg/mL), mixed well, and centrifuged at 15,400 × g for 10 minutes; the supernatant was extracted for injection analysis. Samples with excessive concentrations were diluted before being injected. Dilution method: 100 µL of urine was added to 900 µL of water and mixed well; 100 µL was taken for injection analysis.

Simultaneous Determination of AKF-PD and Its Hydroxylated Metabolites (M1) in Rat Urine

HPLC-UV Conditions

Chromatographic conditions: HPLC ultraviolet detector (Shimadzu LC-2010AHT with LC Solution workstation); chromatographic column (Synergi™ 4 µm Hydro-RP 80 Å 250×4.6 mm, Phenomenex); mobile phase: acetonitrile: 0.1% formic acid aqueous solution = 14.5: 85.5 (v/v) (0–15 mins), acetonitrile: 0.1% formic acid aqueous solution = 40: 60 (v/v) (15.1–22 mins), acetonitrile: 0.1% formic acid aqueous solution = 14.5: 85.5 (v/v) (22.1–26.2 min); flow rate 1.0 mL/min; wavelength 310nm; injection volume 10µL.

Treatment of Samples

A total of 100 µL of rat urine was added to 400 µL of acetonitrile solution (5ug/mL) of carboxylated pirfenidone as an internal standard, mixed well, and centrifuged at 15,400 ×g for 10 minutes. The supernatant was extracted for injection analysis.

Simultaneous Determination of AKF-PD and Its Metabolites (M1 and M2) in Rat Feces

HPLC-UV Conditions

Chromatographic conditions: HPLC ultraviolet detector (Shimadzu LC-2010AHT with LC Solution workstation); chromatographic column (Synergi^TM 4 µm Hydro-RP 80 Å 250x4.6 mm, Phenomenex); mobile phase: acetonitrile 0.1% formic acid aqueous solution = 14.5: 85.5(v/v) (0–21 mins), acetonitrile : 0.1% formic acid aqueous solution = 35: 65 (v/v) (21.1–28 mins), acetonitrile : 0.1% formic acid aqueous solution = 14.5: 85.5 (v/v) (28.1–34 mins); flow rate 1.0 mL/min; wavelength 310 nm; injection volume 10 µL.

Treatment of Fecal Samples

The feces samples of rat taken at 24 hours were stored and weighed at room temperature after drying. They were then soaked in 10 mL of methanol for 10 hours and ground in a mortar, before being extracted with a small amount of methanol several times. The extract was transferred to a 25mL volumetric flask, methanol was added, and the flask was shaken well, before the solution was filtered through a 0.45µm microporous membrane. A total of 100µL of internal standard carboxylated pirfenidone acetonitrile (25µg/mL) was added to 1mL of the filtrate and mixed. The residue was dried under nitrogen flow, dissolved in 100µL of 50% methanol aqueous solution, and centrifuged at 15,400 ×g for 10 minutes. The supernatant was taken for sample analysis.

Results

Dosage

Table 3 shows the basic information and administration information of each experimental animal. The actual dose was equal to the dose given with the remaining dose subtracted. After gavage of the rats, the remaining part of the syringe was washed out with methanol into a 250mL or 500mL volume flask, to which water was added. The flask was shaken well, and 100μL of the solution was added to 400ul of internal standard carboxylated pirfenidone acetonitrile solution (5µg/mL) and mixed well. AKF-PD and its hydroxylated metabolites (M1) were simultaneously detected with 10ul of the mixture through the HPLC-UV. After that, the detection of the residual amount of AKF-PD would be detected.

Table 3 The Content and Total Recovery Rate of AKF-PD and Its Metabolites M1 and M2

Determination of AKF-PD and Its Metabolites in the Urine and Feces of Rats

The content detection results for M1, M2, and AKF-PD in the rat urine and feces samples are shown in Table 3. Flufenidone was mainly excreted in the form of carboxylated metabolites (M2) in rats urin and feces, mainly through kidneys. And the recovery rate of the drug was about 87.07%. There was no statistical difference in total excretion and carboxylated metabolites (M2) between male and female rats (Figure 2).

Figure 2 The amount of excretion in rat urine (μmoL) the total excretion of rats.

Material Balance

Total excretion was calculated as the total amount of AKF-PD and its metabolites M1 and M2 excreted in the urine and feces. Total excretion divided by actual dose and multiplied by 100% was the total recovery. The calculation results are shown in Table 3. The urinary and fecal excretion rates of AKF-PD and its main metabolites M1 and M2 are shown in Table 4.

Table 4 Excretion Rates (%) of AKF-PD and Its Metabolites M1 and M2 in Urine and Feces of Rats

Discussion and Conclusion

AKF-PD is a pyridone compound, which is a newly discovered anti-organ or tissue fibrosis drug. It has a good effect on various organ fibrotic diseases such as liver fibrosis, kidney fibrosis and so on. However, there are few reports on the AKF-PD, metabolites of AKF-PD and the quality control methods of their preparations by combining animal experiments with HPLC-MS at home and abroad. In this paper, experiment combined with HPLC-MS was established to determine the content of AKF-PD in rats after administration. The method was simple, specific, good separation and accurate, it can effectively study the effects of AKF-PD on metabolism and excretion pathway in rats.

After the rats were given AKF-PD intragastrically, 98% of the total excretion was excreted in the form of carboxylated metabolites and there were few prototype drugs and hydroxylated metabolites from the results that combines animal experiments with HPLC-MS. And the main excretion route was kidney excretion, with bile excretion only accounting for approximately 11% of the total excretion. Which was no significant difference between male and female rats. The total recovery rate in this study was 87.07%, below 90%, but the prototype drug excreted from the stool was 0.3% below the dose. In addition, AKF-PD belongs to a compound with high permeability and liposolubility, which is mainly oxidized into 2-hydroxymethyl and 5-carboxyl AKF-PD through the phase I metabolic reaction in rats. Therefore, the influence of liver drug enzyme activity on drugs should be further considered.

The metabolism and excretion mechanism of AKF-PD in rats was studied by substance balance and corresponding mechanism, in order to provide theoretical reference for further study of AKF-PD.